Extracellular vesicles for the treatment of central nervous system diseases

被引:43
|
作者
Gratpain, Viridiane [1 ]
Mwema, Ariane [1 ,2 ]
Labrak, Yasmine [1 ,2 ]
Muccioli, Giulio G. [2 ]
van Pesch, Vincent [3 ,4 ]
des Rieux, Anne [1 ]
机构
[1] Catholic Univ Louvain, Louvain Drug Res Inst, Adv Drug Delivery & Biomat, UCLouvain, B-1200 Brussels, Belgium
[2] Catholic Univ Louvain, Louvain Drug Res Inst, Bioanal & Pharmacol Bioact Lipids, UCLouvain, B-1200 Brussels, Belgium
[3] Catholic Univ Louvain, Inst Neurosci, Neurochem Unit, UCLouvain, B-1200 Brussels, Belgium
[4] Clin Univ St Luc, B-1200 Brussels, Belgium
关键词
miRNA; Nose to brain; Glioblastoma; Neurodegeneration; Neuroinflammation; Surface modification; Nanocarriers; Drug Delivery; Multiple Sclerosis; BLOOD-BRAIN-BARRIER; MESENCHYMAL STROMAL CELLS; CONVECTION-ENHANCED DELIVERY; DRUG-DELIVERY; ALPHA-SYNUCLEIN; IN-VITRO; PARKINSONS-DISEASE; ENDOTHELIAL MICROPARTICLES; ALZHEIMER-DISEASE; MEDIATED TRANSFER;
D O I
10.1016/j.addr.2021.05.006
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The interest in extracellular vesicles (EVs) increased during the last decade. It is now established that these vesicles play a role in the pathogenesis of central nervous system diseases (CNS), which explains why they are studied as biomarkers in these pathologies. On the other hand, EVs can also present ther-apeutic properties, often similar to their parent cells, as observed with mesenchymal stem cell-derived EVs. They can then be used as therapeutics, alone or combined with a bioactive molecule, for the treat-ment of CNS diseases, as they can cross the blood-brain barrier more easily than synthetic nanomedici-nes and are less immunogenic. A few clinical trials are currently on-going but there are still challenges to overcome for further clinical translation such as the scale-up of the production, the lack of standardiza-tion for isolation and characterization methods and the low encapsulation efficiency. (c) 2021 Elsevier B.V. All rights reserved.
引用
收藏
页码:535 / 552
页数:18
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